Effect of Dynamic Cupping Versus Myofascial Release Therapy in Patients With Mechanical Neck Pain

June 23, 2024 updated by: Mohamed Gamal Abouelyazeed Ali, South Valley University

Effect of Dry Cupping Massage Versus Myofascial Release Therapy in Patients With Mechanical Non-specific Neck Pain: a Quasi-experimental Study

A Quasi-experimental study will investigate the effect of dry cupping massage versus myofascial release on patients with mechanical neck pain.

Study Overview

Detailed Description

PURPOSE: To investigate the effect of dry cupping massage versus myofascial release on pain level, range of motion, and functional level in mechanical neck pain…

BACKGROUND: Neck pain is a multivariate disease and is a leading issue in a modernized society. The economic burden of neck pain is remarkable and includes treatment costs, reduced productivity, and job-related problems (Cohen, 2015).

There is no one definitive treatment for neck pain. However, different pharmacological and non-pharmacological treatments have been recommended, including laser therapy, massage, acupuncture, yoga, and aquatic therapy (Corvillo et al., 2020). However, no studies are focusing on comparing the effect of dynamic cupping and myofascial release in mechanical neck pain.

HYPOTHESES: There will be a non-significant difference between dry cupping massage and myofascial release on pain level, range of motion, and functional level in patients with mechanical neck pain…

RESEARCH QUESTION: Will there be a difference between dry cupping massage versus myofascial release on pain level, range of motion, and functional level in patients with mechanical neck pain?

Study Type

Interventional

Enrollment (Estimated)

38

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Cairo, Egypt, 82798
        • Recruiting
        • Faculty of Physical Therapy
        • Contact:
    • Qena
      • Qinā, Qena, Egypt, 83523
        • Recruiting
        • Faculty of physical therapy, South Valley University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Age between 18- 40 years.
  2. Participants have experienced mechanical neck pain for at least the previous 3 months.

Exclusion Criteria:

  • Participants aged below 18 years-old and those above 40 years old
  • Mechanical neck pain due to trauma, disc protrusion, congenital deformity of the spine, spinal stenosis, and rheumatoid disease.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: group A
group A (will receive cupping massage technique in addition to traditional exercises)
Dry cupping is a form of massage therapy that involves using Hijamat cups without skin injury while applying suction and then performing circular and transverse movements
Other Names:
  • traditional exercises (neck stretching and strengthening exercises)
Experimental: Group B
group B (will receive myofascial release technique in addition to traditional exercises)
Myofascial release is a form of manual therapy using hands-on techniques to regain tissue extensibility and elasticity
Other Names:
  • traditional exercises (neck stretching and strengthening exercises)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cervical range of motion
Time Frame: Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
Cervical flexion and extension ranges of motion are measured by goniometer in numerical degrees
Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck Disability index
Time Frame: Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
The neck disability index is a questionnaire has been designed to inform how neck pain has affected different aspects in everyday life.
Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
Visual analog scale
Time Frame: Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
The visual analog scale is a scale for pain severity assessment with range from 0 (o pain) to 10 (intolerable pain)
Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2023

Primary Completion (Estimated)

July 12, 2024

Study Completion (Estimated)

July 20, 2024

Study Registration Dates

First Submitted

August 27, 2023

First Submitted That Met QC Criteria

September 3, 2023

First Posted (Actual)

September 11, 2023

Study Record Updates

Last Update Posted (Actual)

June 25, 2024

Last Update Submitted That Met QC Criteria

June 23, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • cupping vs release

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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